Canonical Allele Identifier: CA1742494538

Gene: GARIN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723300A= , CM000669.2:g.128723300A=	GRCh38
NC_000007.13:g.128363354A= , CM000669.1:g.128363354A=	GRCh37
NC_000007.12:g.128150590A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.791A= MANE Select	ENSP00000477573.2:p.His264=
ENST00000315184.9:c.791A=	ENSP00000326652.4:p.His264=
ENST00000466842.1:c.359A=	ENSP00000417930.1:p.His120=
ENST00000469348.5:n.650A=
ENST00000471558.5:c.791A=	ENSP00000418672.1:p.His264=
ENST00000484425.6:c.362A=	ENSP00000418591.2:p.His121=
ENST00000485070.5:c.494A=	ENSP00000418192.1:p.His165=
ENST00000493738.5:n.747A=
ENST00000621392.4:c.494A=	ENSP00000477573.1:p.His165=
NM_001282788.1:c.791A=	NP_001269717.1:p.His264=
NM_001282789.1:c.494A=	NP_001269718.1:p.His165=
NM_032599.3:c.791A=	NP_115988.1:p.His264=
NR_104242.1:n.891A=
NR_104243.1:n.780A=
XM_017012743.2:c.791A=	XP_016868232.1:p.His264=
XR_002956499.1:n.842A=
NM_001282788.2:c.791A=	NP_001269717.1:p.His264=
NM_001282789.2:c.494A=	NP_001269718.1:p.His165=
NM_032599.4:c.791A=	NP_115988.1:p.His264=
NR_104242.2:n.842A=
NR_104243.2:n.780A=
NM_001282788.3:c.791A= MANE Select	NP_001269717.1:p.His264=